Variant #0000003784 (NC_000001.10:-, FH(NM_000143.3):c.139C>T)
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
Disease-associated missense FH changes map to highly conserved residues, mostly in or around the
e |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
FH_00028 See all 2 reported entries |
Frequency |
- |
Variant remarks |
blood |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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